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Results: 1-8 |
Results: 8
Purine nucleoside phosphorylase inhibitor BCX-1777 (immucillin-H) - a novel potent and orally active immunosuppressive agent
Authors: Bantia, S Miller, PJ Parker, CD Ananth, SL Horn, LL Kilpatrick, JM Morris, PE Hutchison, TL Montgomery, JA Sandhu, JS
Citation: S. Bantia et al., Purine nucleoside phosphorylase inhibitor BCX-1777 (immucillin-H) - a novel potent and orally active immunosuppressive agent, INT IMMUNO, 1(6), 2001, pp. 1199-1210
Comparison of the anti-influenza virus activity of RWJ-270201 with those of oseltamivir and zanamivir
Authors: Bantia, S Parker, CD Ananth, SL Horn, LL Andries, K Chand, P Kotian, PL Dehghani, A El-Kattan, Y Lin, T Hutchison, TL Montgomery, JA Kellog, DL Babu, YS
Citation: S. Bantia et al., Comparison of the anti-influenza virus activity of RWJ-270201 with those of oseltamivir and zanamivir, ANTIM AG CH, 45(4), 2001, pp. 1162-1167
Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity
Authors: Chand, P Kotian, PL Dehghani, A El-Kattan, Y Lin, TH Hutchison, TL Babu, YS Bantia, S Elliott, AJ Montgomery, JA
Citation: P. Chand et al., Systematic structure-based design and stereoselective synthesis of novel multisubstituted cyclopentane derivatives with potent antiinfluenza activity, J MED CHEM, 44(25), 2001, pp. 4379-4392
BCX-1812 (RWJ-270201): Discovery of a novel, highly potent, orally active,and selective influenza neuraminidase inhibitor through structure-based drug design
Authors: Babu, YS Chand, P Bantia, S Kotian, P Dehghani, A El-Kattan, Y Lin, TH Hutchison, TL Elliott, AJ Parker, CD Ananth, SL Horn, LL Laver, GW Montgomery, JA
Citation: Ys. Babu et al., BCX-1812 (RWJ-270201): Discovery of a novel, highly potent, orally active,and selective influenza neuraminidase inhibitor through structure-based drug design, J MED CHEM, 43(19), 2000, pp. 3482-3486
Hydrophobic benzoic acids as inhibitors of influenza neuraminidase
Authors: Atigadda, VR Brouillette, WJ Duarte, F Babu, YS Bantia, S Chand, P Chu, NM Montgomery, JA Walsh, DA Sudbeck, E Finley, J Air, GM Luo, M Laver, GW
Citation: Vr. Atigadda et al., Hydrophobic benzoic acids as inhibitors of influenza neuraminidase, BIO MED CH, 7(11), 1999, pp. 2487-2497
Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping (vol 9, pg 1901, 1999)
Authors: Brouillette, WJ Atigadda, VR Duarte, F Luo, D Air, GM Babu, YS Bantia, S
Citation: Wj. Brouillette et al., Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping (vol 9, pg 1901, 1999), BIOORG MED, 9(22), 1999, pp. 3259-3259
Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping
Authors: Brouillette, WJ Atigadda, VR Luo, M Air, GM Babu, YS Bantia, S
Citation: Wj. Brouillette et al., Design of benzoic acid inhibitors of influenza neuraminidase containing a cyclic substitution for the N-acetyl grouping, BIOORG MED, 9(14), 1999, pp. 1901-1906
Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent
Authors: Atigadda, VR Brouillette, WJ Duarte, F Ali, SM Babu, YS Bantia, S Chand, P Chu, N Montgomery, JA Walsh, DA Sudbeck, EA Finley, J Luo, M Air, GM Laver, GW
Citation: Vr. Atigadda et al., Potent inhibition of influenza sialidase by a benzoic acid containing a 2-pyrrolidinone substituent, J MED CHEM, 42(13), 1999, pp. 2332-2343
Risultati: 1-8 |